Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.
- NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_assertion description "[We identified the missense mutation M520R in the calmodulin binding domain of the Kv7.1 channel from a German family with long QT-syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.
- NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_assertion evidence source_evidence_literature NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.
- NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_assertion SIO_000772 17482572 NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.
- NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_assertion wasDerivedFrom befree-20150227 NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.
- NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_assertion wasGeneratedBy ECO_0000203 NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP279405.RAXrwo_yRVi9g-2yp5WTEAOpL2ZpSJAhb4uzHGycdS9uE130_provenance.